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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5349292translocation1nstd200human GRCh38 chr15: 91,484,561-91,484,561 , GRCh38 chr15: 91,484,441-91,484,441 , GRCh37.p13 chr15: 92,027,671-92,027,671 , GRCh37.p13 chr15: 92,027,791-92,027,791 CRAT37
    nsv5152480mobile element insertion1nstd203human GRCh38 chr15: 91,472,485-91,472,498 , GRCh37.p13 chr15: 92,015,715-92,015,728 CRAT37
    nsv4856345copy number variation1nstd200human GRCh37 chr15: 92,027,671-92,027,791 , GRCh38.p12 chr15: 91,484,441-91,484,561 CRAT37
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4568637mobile element insertion1nstd166human GRCh37.p13 chr15: 92,027,530-92,027,530 , GRCh38.p12 chr15: 91,484,300-91,484,300 CRAT37
    nsv4567963mobile element insertion1nstd166human GRCh37.p13 chr15: 92,023,761-92,023,761 , GRCh38.p12 chr15: 91,480,531-91,480,531 CRAT37
    nsv4511069mobile element insertion1nstd166human GRCh37.p13 chr15: 92,012,027-92,012,027 , GRCh38.p12 chr15: 91,468,797-91,468,797 CRAT37, LOC107984778
    nsv4502434mobile element insertion1nstd166human GRCh37.p13 chr15: 92,016,068-92,016,068 , GRCh38.p12 chr15: 91,472,838-91,472,838 CRAT37
    nsv4500184mobile element insertion1nstd166human GRCh37.p13 chr15: 92,028,292-92,028,292 , GRCh38.p12 chr15: 91,485,062-91,485,062 CRAT37
    nsv4456778copy number variation1nstd102humanPathogenic GRCh37 chr15: 91,229,877-93,677,014 , GRCh38.p12 chr15: 90,686,646-93,133,785 H2AZ2P1, MAN2A2, 44 more genes
    nsv4456430copy number variation1nstd102humanPathogenic GRCh37 chr15: 90,288,175-102,429,112 , GRCh38.p12 chr15: 89,744,944-101,888,909 IQGAP1, LOC400464, 210 more genes
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
    nsv4350274copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614 AKAP13, LOC105370972, 184 more genes
    nsv4251880copy number variation1nstd166human GRCh37.p13 chr15: 92,022,991-92,023,060 , GRCh38.p12 chr15: 91,479,761-91,479,830 CRAT37
    nsv4250302copy number variation1nstd166human GRCh37.p13 chr15: 92,020,632-92,023,764 , GRCh38.p12 chr15: 91,477,402-91,480,534 CRAT37
    nsv4245683copy number variation1nstd166human GRCh37.p13 chr15: 91,637,900-92,049,000 , GRCh38.p12 chr15: 91,094,670-91,505,770 SV2B, LOC107984778, 2 more genes
    nsv4239025copy number variation1nstd166human GRCh37.p13 chr15: 91,930,379-92,020,276 , GRCh38.p12 chr15: 91,387,149-91,477,046 CRAT37, LOC107984778
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3920352copy number variation1nstd102humanPathogenic GRCh38 chr15: 83,711,377-101,843,270 , NCBI36 chr15: 82,171,133-100,200,996 , GRCh37 chr15: 84,380,129-102,383,473 LOC102724465, SNRPA1, 333 more genes
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